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作 者:吉鹏[1] 刘红飞[1] 王朝生[1] 陈向玲[1] 王华平[1]
机构地区:[1]东华大学材料科学与工程学院纤维材料改性国家重点实验室,上海201620
出 处:《合成纤维工业》2015年第1期1-6,共6页China Synthetic Fiber Industry
基 金:国家科技支撑计划项目(2011BAE05B01)
摘 要:通过共聚反应合成了含不同相对分子质量聚乙二醇(PEG)及其添加量的聚对苯二甲酸乙二醇酯(PET)-PEG嵌段共聚物,经熔融纺丝制备PET—PEG共聚酯纤维。利用核磁共振氢谱、差示扫描量热分析、X射线衍射(XRD)等手段对共聚酯的结构及其热性能进行了表征。结果表明:核磁共振氢谱证实了共聚酯为PET—PEG目标产物;随着PEG相对分子质量从800增加到6000,PET—PEG共聚酯的熔融温度从243.97℃增加到253.55℃,冷却结晶温度从176.32℃增加到189.25℃,表面接触角从74.2°下降到62.3°,共聚酯纤维在标准环境下的回潮率从0.51%增加到0.68%;在PEG相对分子质量为2000时,添加PEG相对对苯二甲酸(PTA)质量分数为0~20%时,共聚酯的熔融温度与冷却结晶温度随着PEG添加量的增加呈下降趋势,共聚酯纤维的回潮率呈指数增加;PEG添加量相对PTA质量分数为20%时,共聚酯可纺性较差;XRD表明PEG在结晶过程中并不进入PET晶格中,为了保证共聚酯的良好吸湿性能和力学性能,PET—PEG的共聚合反应时,PEG适宜的相对分子质量为2000,添加量相对PTA的质量分数为10%。The block copolyesters of polyethylene terephthalate-polyethylene glycol (PET-PEG) with different amounts of PET with different relative molecular mass were synthesized by copolymerization reaction and were spun into PET-PEG copolyester fibers by melt spinning process. The structure and thermal properties of the copolyesters were characterized by nuclear magnetic resonance, differential scanning Calorimetry and X-ray diffraction analysis (XRD). The results showed that PET-PEG copolyester was proved to be the target product by nuclear magnetic resonance; the PET-PEG copolyester had the melting temperature increasing from 243.97 ℃ to 253.55 ℃ ,the cold crystal!ization temperature increasing from 176.32 ℃ to 189.25 ℃ and the surface contact angle decreasing from 74.2° to 62.3°and the copolyester fibers had the moisture regain increasing from 0.51% to 0. 68% under standard environment when the relative molecular mass of PEG was increased from 800 to 6 000; the melting temperature and cold crystallization temperature of the copolyesters appeared a downward tendency and the moisture regain of the copolyester fibers showed an exponential increase with the addition of PEG with the relative molecular mass of 2 000 from 0 to 20 % by mass fraction based on purified terephthalic acid (PTA) ; the spinnability of the copolyesters was poor as the mass fraction of PEG was 20% based on PTA ; PEG did not enter the crystal lattice of PET during the crystallization process ; and the relative molecular mass of PEG should be 2 000 and the addition of PEG should be 10% by mass fraction based on PTA in order to acquire the favorable moisture absorption and mechanical properties of the copolyesters during the copolymerization reaction of PET-PEG.
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